Background: Intraoperative hemolysis and inflammation are associated with acute kidney injury (AKI) following cardiac surgery. Plasma-free hemoglobin induces heme oxygenase-1 (HO-1) expression. HO-1 degrades heme but increases in experimental models of AKI. This study tested the hypothesis that plasma HO-1 concentrations are associated with intraoperative hemolysis and are increased in patients that develop AKI following cardiac surgery. Methods: We measured plasma HO-1, free hemoglobin, and inflammatory markers in 74 patients undergoing cardiopulmonary bypass (CPB). AKI was defined as an increase in serum creatinine concentration of 50% or 0.3 mg/dl within 72 h of surgery. Results: Twenty-eight percent of patients developed AKI. HO-1 concentrations increased from 4.2 +/- 0.2 ng/ml at baseline to 6.6 +/- 0.5 ng/ml on postoperative day (POD) 1 (p < 0.001). POD1 HO-1 concentrations were 3.1 ng/ml higher (95% CI 1.1-5.1) in AKI patients, as was the change in HO-1 from baseline to POD1 (4.4 1.3 ng/ml in AKI patients vs. 1.5 +/- 0.3 ng/ml in no-AKI patients, p = 0.006). HO-1 concentrations remained elevated in AKI patients even after controlling for AKI risk factors and preoperative drug therapy. Peak-free hemoglobin concentrations correlated with peak HO-1 concentrations on POD1 in patients that developed AKI (p = 0.02). Duration of CPB and post-CPB IL-6 and IL-10 concentrations were also associated with increased HO-1 on POD1. Conclusion: Plasma HO-1 is increased in patients that develop AKI, and CPB duration, hemolysis, and inflammation are associated with increased HO-1 concentrations following cardiac surgery. Strategies that alter hemolysis and HO-1 expression during cardiac surgery may affect risk for AKI. (c) 2014S. Karger AG, Basel
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Univ Mississippi, Med Ctr, Dept Physiol & Biophys, Mississippi Ctr Obes Res, Jackson, MS 39216 USAUniv Mississippi, Med Ctr, Dept Physiol & Biophys, Mississippi Ctr Obes Res, Jackson, MS 39216 USA
Drummond, Heather A.
Mitchell, Zachary L.
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Univ Mississippi, Med Ctr, Dept Physiol & Biophys, Mississippi Ctr Obes Res, Jackson, MS 39216 USAUniv Mississippi, Med Ctr, Dept Physiol & Biophys, Mississippi Ctr Obes Res, Jackson, MS 39216 USA
Mitchell, Zachary L.
Abraham, Nader G.
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New York Med Coll, Dept Med, Valhalla, NY 10595 USA
New York Med Coll, Dept Pharmacol, Valhalla, NY 10595 USA
Marshall Univ, Joan C Edwards Sch Med, Huntington, WV 25701 USAUniv Mississippi, Med Ctr, Dept Physiol & Biophys, Mississippi Ctr Obes Res, Jackson, MS 39216 USA
Abraham, Nader G.
Stec, David E.
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Univ Mississippi, Med Ctr, Dept Physiol & Biophys, Mississippi Ctr Obes Res, Jackson, MS 39216 USAUniv Mississippi, Med Ctr, Dept Physiol & Biophys, Mississippi Ctr Obes Res, Jackson, MS 39216 USA
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Univ Alabama Birmingham, Dept Med, Div Nephrol, Nephrol Res & Training Ctr, Birmingham, AL 35294 USAUniv Alabama Birmingham, Dept Med, Div Nephrol, Nephrol Res & Training Ctr, Birmingham, AL 35294 USA
Zarjou, Abolfazl
Agarwal, Anupam
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Univ Alabama Birmingham, Dept Med, Div Nephrol, Nephrol Res & Training Ctr, Birmingham, AL 35294 USA
Dept Vet Affairs Med Ctr, Birmingham, AL USAUniv Alabama Birmingham, Dept Med, Div Nephrol, Nephrol Res & Training Ctr, Birmingham, AL 35294 USA